Chapter 22: Q30P (page 1173)
Show how octane-2,7-dione might cyclize to a cycloheptenone. Explain why ring closure to the cycloheptenone is not favored.
Chapter 22: Q30P (page 1173)
Show how octane-2,7-dione might cyclize to a cycloheptenone. Explain why ring closure to the cycloheptenone is not favored.
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Get started for freePropose a mechanism for the acid-catalyzed bromination of pentan-3-one.
Many of the condensations we have studied are reversible. The reverse reactions are often given the prefix retro-, the Latin word meaning “backward.” Propose mechanisms to account for the following reactions.
a.
b.
c.
d.
Show how you would accomplish the following conversions in good yields. You may use any necessary reagents.
Question: Predict the products of the following reactions
c.
Predict the products of the following reactions.
a. Cyclopentanone +Br2 in acetic acid
b. 1phenylethanol + I2 excess
c.
d)
e)
f)
g)
h)
i)
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